HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-methylpiperazine-1-carbonyl)benzoic Acid → 1-(4-(6-((Dimethylamino)methyl)-4-morpholinopyrrolo[2,1-f][1,2,4]triazin-2-yl)phenyl)-3-(4-(4-methylpiperazine-1-carbonyl)phenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-methylpiperazine-1-carbonyl)benzoic Acid | HCID 2051417 | — |
| Reactant | HCID 117987912 | HCID 117987912 | — |
| Reactant | HCID 117988374 | HCID 117988374 | — |
| Product | 1-(4-(6-((Dimethylamino)methyl)-4-morpholinopyrrolo[2,1-f][1,2,4]triazin-2-yl)phenyl)-3-(4-(4-methylpiperazine-1-carbonyl)phenyl)urea | HCID 72549104 | 15.1% |
Reaction Steps
According to the general methods described in example 13, 4-(4-methylpiperazine-1-carbonyl)benzoic acid was used as starting material, and the resulting 4-(4-methylpiperazine-1-carbonyl)benzoyl azide reacted with 13a to give a white solid (9 mg, 15.1%). 1H NMR (300 MHz, DMSO-d6): δ 9.63 (br, s, 2H), 8.16 (d, J=8.9 Hz, 2H), 7.92 (s, 1H), 7.57 (d, J=8.9 Hz, 2H), 7.53 (d, J=8.5 Hz, 2H), 7.34 (d, J=8.5 Hz, 2H), 7.13 (s, 1H), 4.07 (br, s, 6H), 3.80 (br, s, 4H), 3.51 (br, s, 4H), 3.06 (br s, 2H), 2.55 (s, 6H), 2.38 (br s, 2H), 2.24 (s, 3H). ESI-MS: 598 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447101B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-74cbe61f66974864af3f503e3f73580d |
| Source note | uspto-grants-2016_09 |